Allele Registry

Canonical Allele Identifier: PA093487

Gene: AVP HGNC NCBI

ClinVar RCV:

RCV000013002

ClinVar Variation:

12218

HGVS (amino-acid)	Matching Registered Transcripts
NP_000481.2:p.Val67Ala	CA121972 NM_000490.5:c.200T>C